FDA UDI In Commercial Distribution 🇺🇸 United States

LX9max

DI: 08809802644892 · Model: LX9M100-LLZ · DAESUNG MAREF CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LX9max
Primary DI
08809802644892
Version / Model
LX9M100-LLZ
Company Name
DAESUNG MAREF CO.,LTD.
Labeler DUNS
688817949
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-14
Public Version
1
Public Version Date
2025-11-24
Public Version Status
New
Public Device Record Key
96cc14c3-a9f4-4dc9-afcd-d78e346d29e3

Device Description

Main Device 1ea, Leg Sleeve (L) 2ea, Leg Sleeve (XXL) 2ea, Double Tubing 1ea [One Set Box]

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IRP Massager, Powered Inflatable Tube

GMDN Terms

Code Name
44785 Sequential venous compression system inflator

Identifiers

Type ID
Package 18809802644899
Primary 08809802644892

Premarket Submissions

Submission Number Supplement Number
K203498 000